Several studies suggest fully-automated ventilation to ventilate with a lower amount of MP in unselected ICU patients, patients after cardiac surgery, and patients with and without ARDS. The current study will directly compare the amount of MP in invasively ventilated critically ill patients by calculating MP breath-by-breath, using the various equations proposed in the literature.
Rationale: Mechanical ventilation can cause ventilator-induced lung injury (VILI). Lung protective ventilation, consisting of a low tidal volume (VT), a low plateau pressure (Pplateau) and a low driving pressure (ΔP) improves survival and shortens duration of ventilation in patients with acute respiratory distress syndrome (ARDS). Lung protective ventilation may also benefit critically ill patients with respiratory failure not caused by ARDS. 'Mechanical Power of ventilation' (MP), the amount of energy per time transferred from the ventilator to the respiratory system, is a summary variable that includes all the components that play a role in VILI. With fully-automated closed-loop ventilation, these components are no longer set by the operator, but under control of the algorithms in the ventilator. Objective: To compare MP under INTELLiVENT-adaptive support ventilation (ASV), a fully-automated closed-loop ventilation, with MP under conventional ventilation. Hypothesis: INTELLiVENT-ASV compared to conventional ventilation results in a lower MP. Study design: National, multicenter, crossover, randomized clinical trial. Study population: Invasively ventilated critically ill patients. Methods: The ventilator will be randomly switched between INTELLiVENT-ASV for 3 hours and conventional ventilation for 3 hours. The amount of MP is calculated using various equations proposed in the literature. Study endpoints: The primary endpoint is the amount of MP with each form of invasive ventilation. Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Differences in burden and risks of the two ventilation strategies compared in the current study are not expected. Both modes of ventilation are interchangeably used as part of standard care in the participating centers. No other interventions are performed. Neither the collection of demographic and outcome data, nor the capturing of ventilation characteristics causes harm to patients.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
96
With INTELLiVENT-ASV, the patient's conditions, 'ARDS', 'Chronic Hypercapnia' or 'Traumatic Brain Injury' can be chosen, if applicable. The controllers for minute volume, PEEP and FiO2 are all activated, and the target shifts for etCO2 and SpO2 are adjusted, if necessary.
With conventional ventilation, the same etCO2 and SpO2 levels are targeted as with INTELLiVENT-ASV, but here the caregiver is fully responsible for choosing the settings.
Academic Medical Center
Amsterdam, North Holland, Netherlands
Reinier de Graaf Gasthuis
Delft, Netherlands
Dijklander Ziekenhuis
Hoorn, Netherlands
The amount of MP delivered with each form of invasive ventilation
The amount of MP delivered with INTELLiVENT-ASV and conventional ventilation
Time frame: 3 hours per ventilation mode
Duration of ventilation
Duration of ventilation in survivors
Time frame: first 28 days after start of ventilation
ICU-length and hospital of stay
Length of stay in the intensive care unit and in the hospital
Time frame: first 28 days after start of ventilation
28 day-mortality
Any death during ICU-, hospital-stay and within 28 days
Time frame: first 28 days after start of ventilation
Tidal volume
Tidal volume in ml/kg
Time frame: 3 hours per ventilation mode
Respiratory rate
Respiratory rate per minute
Time frame: 3 hours per ventilation mode
Pmax
Maximum airway pressure in cmH2O
Time frame: 3 hours per ventilation mode
Driving pressure
Difference between end-inspiratory pressure and total Positieve End Expiratory Pressure in cmH2O
Time frame: 3 hours per ventilation mode
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